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Search Results for: Hereditary Genetics
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Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk
A functional single nucleotide polymorphism at the promoter region of cyclin A2 is associated with increased risk of colon, liver, and lung cancers
Validation of Genetic Sequence Variants as Prognostic Factors in Early Stage Head and Neck Squamous Cell Cancer Survival
Genome-Wide Gene-Environment Study Identifies Glutamate Receptor Gene GRIN2A as a Parkinson’s Disease Modifier Gene via Interaction with Coffee
Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
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